Canonical Allele Identifier: PA105619
Gene: RYR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000531.2:p.Arg4893Trp
CA024220
NM_000540.3:c.14677C>T